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Potent bisphosphonate therapy for preventing fractures after denosumab discontinuation in osteoporosis: A GRADE-assessed systematic review and meta-analysis

Shah A, Khan S, Rizvi SVZ, Farhan K, Uddin M, Rizvi SUA, Fatima S, Karan AR et al.

Medicine, 2026

683 participants

Abstract

Background: Denosumab cessation causes rebound bone turnover, fast bone loss, and an elevated risk of vertebral fractures. Pooled data about the fracture prevention efficacy of potent bisphosphonates (BPs) as sequential therapy have been lacking to counteract this risk.

Methods: This systematic review and meta-analysis was carried out according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses 2020 guidelines. PubMed, Scopus, the Cochrane Library, and ClinicalTrials.gov were searched from the beginning through May 1, 2026. Included studies comprised adults with osteoporosis or low bone mass who discontinued denosumab and subsequently received potent BP therapy, defined as alendronate or zoledronic acid, compared with no subsequent antiresorptive therapy or a selective estrogen receptor modulator (SERM). Random-effects meta-analyses were performed using the Mantel-Haenszel method to calculate pooled risk ratios (RRs) with 95% confidence intervals (CIs). Prespecified subgroup analyses were conducted based on comparator type. The Grading of Recommendations Assessment, Development and Evaluation assessment method was applied to assess the certainty of the evidence.

Results: Six studies were included; 683 participants contributed to the primary incident vertebral fracture analysis. Potent BP therapy was linked to a considerable reduction in incident vertebral fractures (RR = 0.29; 95% CI: 0.14-0.59; 71% relative risk reduction), multiple vertebral…

How strong is the evidence?

Evidence Hub reads this as a meta-analysis, done in people. Its evidence level is 1 of 5 (Highest · pooled evidence). Pooled evidence from several studies sits at the top of the evidence pyramid. Reported size: 683 participants or records.

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